Abstract
We report on the size-dependent interaction of carbon monoxide molecules with hydrogen covered vanadium clusters containing between 5 and 20 atoms. Structural information on these hydrogen covered vanadium clusters and their complexes with CO is obtained from infrared multiple photon dissociation spectroscopy, complemented with density functional theory calculations for the V-5 to V-9 cluster sizes. The non-dissociative or dissociative binding of CO on the metal clusters is detected by the presence or absence of the nu(CO) stretching band in the infrared spectra. It is found that the CO molecule dissociates on bare vanadium clusters, while it adsorbs intact on all saturated hydrogen covered V-5-20(+) clusters, with the distinctive exceptions of V-5(+), V-9(+), V-11(+), and V-19(+). We show that dissociative chemisorption is prevented when the potential binding sites of atomic C and O atoms are blocked by H atoms.
Original language | English |
---|---|
Pages (from-to) | 2516-2520 |
Number of pages | 5 |
Journal | Journal of the American Chemical Society |
Volume | 129 |
Issue number | 9 |
DOIs | |
Publication status | Published - 7 Mar 2007 |
Keywords
- DEUTERIDE BOND-ENERGIES
- GUIDED ION-BEAM
- APPROXIMATE COULOMB POTENTIALS
- AUXILIARY BASIS-SETS
- METAL-CLUSTERS
- ELECTRONIC-STRUCTURE
- CHEMICAL PROBE
- IRON CLUSTERS
- D-2
- SPECTROSCOPY